GE Inspection Technologies, LP: Medical Device Recall in 2014 - (Recall #: Z-0426-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2014.

Data Source: FDA.

Product Description:

GE Cabinet X-ray systems

Product Classification:

Class II

Date Initiated: November 10, 2014

Date Posted: December 24, 2014

Recall Number: Z-0426-2015

Event ID: 69846

Reason for Recall:

GE discovered these cabinet x-ray systems' potential failure to comply with the Cabinet X-ray System performance standards.

Status: Terminated

Product Quantity: 11

Code Information:

XXL cabinet x-ray systems, serial numbers A586590 and A586780; xlcube compact cabinet x-ray systems, serial numbers A583730, A586430, and A586460; a VTOMEX C450 cabinet x-ray system, serial number VTXO1JOOO2-2245 14; VTOMEX L300 cabinet x-ray systems, serial numbers VTX01lF007-208813, VTX01F007-196312 and VTXO1FOO07-1946 12; and VTOMEX L450 cabinet x-ray systems, serial numbers VTXO1K0001-184711 and PX_10E000-179013.

Distribution Pattern:

US Distribution to the states of MI, PA, NH, CA, OR, WA, NC, IN and SC.

Voluntary or Mandated:

Voluntary: Firm initiated